| 疾病名称 |
别名 |
|
| Capillary Malformation-Arteriovenous Malformation 1 |
|
Parkes Weber Syndrome
|
Capillary Malformation-Arteriovenous Malformation
|
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Capillary Malformation-Arteriovenous Malformation Syndrome
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CMAVM1
|
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Cmavm
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Cm-Avm Syndrome
|
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Pkws
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Cm-Avm
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Parkes-Weber Syndrome
|
Capillary Malformation-Arteriovenous Malformation, Type 1
|
|
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| Basal Cell Carcinoma 1 |
|
Basal Cell Carcinoma, Susceptibility To, 1
|
Basal Cell Carcinoma
|
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BCC1
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BCC
|
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Multiple Basal Cell Carcinoma
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Non-Syndromic Basal Cell Carcinoma
|
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Carcinoma, Basal Cell, Susceptibility To, Type 1
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Experimental Organism Basal Cell Carcinoma
|
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Basal Cell Carcinoma, Multiple
|
|
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| Basal Cell Carcinoma, Multiple |
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Multiple Basal Cell Carcinoma
|
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| Klippel-Trenaunay-Weber Syndrome |
|
Klippel-Trenaunay Syndrome
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KTS
|
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Ktw Syndrome
|
Angioosteohypertrophy Syndrome
|
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Angio-Osteohypertrophy Syndrome
|
Klippel Trenaunay Syndrome
|
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Klippel-Trénaunay-Weber Syndrome
|
Haemangiectatic Hypertrophy
|
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Weber-Klippel-Trenaunay
|
Congenital Dysplastic Angiopathy
|
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Klippel-Trenaunay Disease
|
Weber Klippel Trenaunay
|
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| Hereditary Hemorrhagic Telangiectasia |
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Rendu-Osler-Weber Disease
|
Hht
|
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Osler-Weber-Rendu Disease
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Telangiectasia, Hereditary Hemorrhagic
|
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Osler Hemorrhagic Telangiectasia Syndrome
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Orw Disease
|
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Osler Weber Rendu Syndrome
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Osler-Rendu-Weber Disease
|
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Osler-Weber-Rendu Syndrome
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Rendu-Osler Disease
|
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Telangiectasia Hereditary Hemorrhagic
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Telangiectasia Hemorrhagic, Hereditary
|
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Hht - [Hereditary Haemorrhagic Telangiectasia]
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Osler Haemorrhagic Telangiectasia Syndrome
|
|
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| Angioosteohypertrophic Syndrome |
|
Klippel-Trenaunay-Weber Syndrome
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Haemangiectatic Hypertrophy
|
|
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| Telangiectasia, Hereditary Hemorrhagic, Type 1 |
|
Orw Disease
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HHT1
|
|
Hht
|
Telangiectasia, Hereditary Hemorrhagic, Of Rendu, Osler, And Weber
|
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Osler-Rendu-Weber Disease
|
Telangiectasia, Hereditary Hemorrhagic, 1
|
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Hereditary Hemorrhagic Telangiectasia Of Rendu, Osler, And Weber
|
Orw1
|
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Osler-Rendu-Weber Syndrome
|
Osler-Rendu-Weber Syndrome 1
|
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Telangiectasia Hemorrhagic, Hereditary, Type 1
|
Hereditary Hemorrhagic Telangiectasia
|
|
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| Hemangioma, Capillary Infantile |
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HCI
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Capillary Infantile Hemangioma
|
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Hemangioma, Hereditary Capillary
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Hemangioma, Capillary Infantile, Susceptibility To
|
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Hemangioma, Capillary Infantile, Somatic
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Hemangioma Hereditary Capillary
|
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| Weber Syndrome |
|
Midbrain Stroke Syndromes
|
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| Arteriovenous Malformation |
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Arteriovenous Malformations
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Arteriovenous Hemangioma
|
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Cirsoid Aneurysm
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Racemose Aneurysm
|
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Racemose Angioma
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Racemose Hemangioma
|
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Congenital Arteriovenous Malformation
|
|
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| Sturge-Weber Syndrome |
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SWS
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Encephalotrigeminal Angiomatosis
|
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Encephalofacial Angiomatosis
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Sturge-Weber-Dimitri Syndrome
|
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Sturge-Weber-Krabbe Syndrome
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Fourth Phacomatosis
|
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Leptomeningeal Angiomatosis
|
Meningeal Capillary Angiomatosis
|
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Sturge-Weber-Krabbe Angiomatosis
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Sturge-Weber Syndrome, Somatic, Mosaic
|
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Sws Type I - Facial And Leptomeningeal Angiomas
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Sws Type Ii - Facial Angioma Alone, No Cns Involvement
|
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Sws Type Iii - Isolated Leptomeningeal Angiomas
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Sturge Weber Syndrome
|
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Angiomatosis Aculoorbital-Thalamic Syndrome
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Encephalofacial Hemangiomatosis
|
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Encephalofacial Hemangiomatosis Syndrome
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Meningo-Oculo-Facial Angiomatosis
|
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Meningofacial Angiomatosis-Cerebral Calcification Syndrome
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Neuroretinoangiomatosis
|
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Phakomatosis, Sturge-Weber
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Weber-Sturge-Dimitri Syndrome
|
|
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| Stork Bite |
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Salmon Patch Nevus
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Unna'S Nevus
|
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| Neurofibromatosis |
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Neurofibromatoses
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Acoustic Neurofibromatosis
|
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Central Neurofibromatosis
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Peripheral Neurofibromatosis
|
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Recklinghausen'S Neurofibromatosis
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Von Reklinghausen Disease
|
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Neurofibromatosis Type 1
|
|
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| Neurofibromatosis, Type I |
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Von Recklinghausen Disease
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Neurofibromatosis 1
|
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Neurofibromatosis, Type 1
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NF1
|
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Neurofibromatosis, Peripheral Type
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Neurofibromatosis Type I
|
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Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion
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Familial Spinal Neurofibromatosis
|
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Fsnf
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Peripheral Neurofibromatosis
|
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Von Recklinghausen'S Neurofibromatosis
|
Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion
|
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Neurofibromatosis Peripheral Type
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Von Recklinghausen Syndrome
|
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Neurofibromatosis Type 1
|
Von Recklinghausen Neuropathy
|
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Nf1 - [Neurofibromatosis Type 1]
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Recklinghausen Disease
|
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| Angiokeratoma Circumscriptum |
|
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| Lung Squamous Cell Carcinoma |
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Squamous Cell Carcinoma Of Lung
|
Squamous Cell Lung Carcinoma
|
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Epidermoid Cell Carcinoma Of The Lung
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Squamous Cell Lung Cancer
|
|
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| Venous Malformations, Multiple Cutaneous And Mucosal |
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VMCM
|
Multiple Cutaneous And Mucosal Venous Malformations
|
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Mucocutaneous Venous Malformations
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Vmcm1
|
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Cutaneous And Mucosal Venous Malformation
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Dominantly Inherited Venous Malformations
|
|
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| Trophoblastic Neoplasm |
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Trophoblastic Tumor
|
Trophoblastic Neoplasms
|
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| Hemangioma Of Intra-Abdominal Structure |
|
Hemangioma Of Intra-Abdominal Structures
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Hemangioma, Intra-Abdominal
|
|
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| Lymphatic Malformation 12 |
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Central Conducting Lymphatic Anomaly
|
LMPHM12
|
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Ccla
|
Lymphatic Malformation-7
|
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Doid:0081030
|
|
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| Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi |
|
Cloves Syndrome
|
Clove Syndrome
|
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Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, And Skeletal/Spinal Abnormalities
|
Clove Syndrome, Somatic
|
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Nevus
|
Congenital Lipomatous Overgrowth - Vascular Malformation - Epidermal Nevi
|
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Congenital Lipomatous Overgrowth-Vascular Malformation-Epidermal Nevi-Skeletal Anomaly Syndrome
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Congenital Lipomatous Overgrowth-Vascular Malformation-Epidermal Nevi-Spinal Anomaly Syndrome
|
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CLOVE
|
Congenital Lipomatous Overgrowth Vascular Malformations Epidermal Nevi And Skeletal/Spinal Abnormalities
|
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Congenital Arteriovenous Malformation
|
Arteriovenous Hemangioma
|
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Melanocytic Nevus
|
Benign Melanocytic Nevus
|
|
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| Cardiovascular Organ Benign Neoplasm |
|
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| Proteus Syndrome |
|
Proteus Syndrome, Somatic
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Partial Gigantism-Nevi-Hemihypertrophy-Macrocephaly Syndrome
|
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Gigantism, Partial, Of Hands And Feet, Nevi, Hemihypertrophy, And Macrocephaly
|
Wiedemann'S Syndrome
|
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Hemihypertrophy And Macrocephaly
|
Partial Gigantism Of Hands And Feet, Nevi, Hemihypertrophy, Macrocephaly
|
|
Ps
|
PROTEUSS
|
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Partial Gigantism Of Hands And Feet Nevi Hemihypertrophy And Macrocephaly
|
|
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| Basal Cell Carcinoma |
|
Basal Cell Cancer
|
Basal Cell Neoplasm
|
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Basal Cell Carcinoma Of Skin
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Malignant Basal Cell Tumor
|
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Basal Cell Tumor
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Epithelioma Basal Cell
|
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Malignant Basal Cell Neoplasm
|
Rodent Ulcer
|
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Carcinoma Basal Cell
|
Neoplasms, Basal Cell
|
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Basal Cell Carcinomas
|
Experimental Organism Basal Cell Carcinoma
|
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Nodulo-Ulcerative Basal Cell Carcinoma
|
Basalioma
|
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Basal Cell Epithelioma Of Skin
|
Bcc - [Basal Cell Carcinoma] Of Skin
|
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Rodent Ulcer Of Skin
|
Rodent Ulcer Of Unspecified Site
|
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Basal Cell Epithelioma Of Unspecified Site
|
|
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| Cowden Syndrome 1 |
|
Bannayan-Riley-Ruvalcaba Syndrome
|
Pten Hamartoma Tumor Syndrome
|
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Lhermitte-Duclos Disease
|
Bannayan-Zonana Syndrome
|
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Phts
|
Riley-Smith Syndrome
|
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Bzs
|
Ruvalcaba-Myhre-Smith Syndrome
|
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Multiple Hamartoma Syndrome
|
Rmss
|
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Brrs
|
Dysplastic Gangliocytoma Of The Cerebellum
|
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CWS1
|
Cs
|
|
Cd
|
Mham
|
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Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
|
Macrocephaly Multiple Lipomas And Hemangiomata
|
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Bannayan-Ruvalcaba-Riley Syndrome
|
Myhre-Riley-Smith Syndrome
|
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LDD
|
Cerebelloparenchymal Disorder Vi
|
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Hamartoma Syndrome, Multiple
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Bbrs
|
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Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata
|
Macrocephaly, Multiple Lipomas, And Hemangiomata
|
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Macrocephaly Pseudopapilledema And Multiple Hemangiomas
|
Ruvalcaba -Myhre-Smith Syndrome
|
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Ruvalcaba-Myhre Syndrome
|
Cowden Disease
|
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Macrocephaly Pseudopapilledema And Multiple Hemangiomata
|
Cerebellar Granule Cell Hypertrophy And Megalencephaly
|
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Cpd6
|
Pten Hamartoma Tumor Syndromes
|
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Cowden Syndrome, Type 1
|
|
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| Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrome |
|
Juvenile Polyposis-Hereditary Hemorrhagic Telangiectasia Syndrome
|
JPHT
|
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Jp/Hht Syndrome
|
Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia
|
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Jps/Hht
|
Telangiectasia, Hereditary Hemorrhagic, With Juvenile Polyposis Coli
|
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Polyposis, Generalized Juvenile, With Pulmonary Arteriovenous Malformation
|
Jp-Hht
|
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JP/HHT
|
Polyposis, Juvenile/Hereditary Hemorrhagic Telangiectasia Syndrome
|
|
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| Taylor'S Syndrome |
|
Pelvic Congestion Syndrome
|
Congestion-Fibrosis Syndrome
|
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Taylor Syndrome
|
|
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| Capillary Hemangioma |
|
Infantile Hemangioma
|
Strawberry Nevus Of Skin
|
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Cellular Hemangioma Of Infancy
|
Congenital Vascular Hamartoma
|
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Congenital Vascular Naevus
|
Juvenile Hemangioma
|
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Strawberry Haemangioma
|
Strawberry Nevus
|
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Hemangioma Capillary
|
Hemangioma, Capillary
|
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Hemangioma, Cavernous
|
|
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| Noonan Syndrome With Multiple Lentigines |
|
Leopard Syndrome
|
Multiple Lentigines Syndrome
|
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Moynahan Syndrome
|
Cardiomyopathic Lentiginosis
|
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Progressive Cardiomyopathic Lentiginosis
|
Cardio-Cutaneous Syndrome
|
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Lentiginosis Profusa
|
Capute-Rimoin-Konigsmark-Esterly-Richardson Syndrome
|
|
Generalized Lentiginosis
|
Gorlin Syndrome Ii
|
|
Lentiginosis Profusa Syndrome
|
Lentigines, Electrocardiographic Conduction Abnormalities, Ocular Hypertelorism, Pulmonic Stenosis, Abnormal Genitalia, Retardation Of Growth, Deafnes
|
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Diffuse Lentiginosis
|
Nsml
|
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Familial Multiple Lentigines Syndrome
|
Alopecia-Epilepsy-Intellectual Disability Syndrome, Moynahan Type
|
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Progressive Cardiomyopathic Lentiginosis Syndrome
|
Alopecia Epilepsy Oligophrenia Syndrome Of Moynahan
|
|
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| Uterine Corpus Endometrial Carcinoma |
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
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| Arteriovenous Malformations Of The Brain |
|
Cerebral Arteriovenous Malformation
|
Intracranial Arteriovenous Malformation
|
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Intracranial Hemorrhage In Brain Cerebrovascular Malformations, Susceptibility To
|
Intracranial Arteriovenous Malformations
|
|
Bavm
|
Cerebral Arteriovenous Malformations
|
|
Intracranial Hemorrhage In Brain Cerebrovascular Malformations
|
Arteriovenous Malformation Of The Brain, Somatic
|
|
Intracranial Avm
|
Arteriovenous Malformations Cerebral
|
|
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| Intracranial Cavernous Angioma |
|
Intracranial Cavernoma
|
Intracranial Cavernous Hemangioma
|
|
|
| Intracranial Structure Hemangioma |
|
Angioma Of Intracranial Structure
|
Hemangioma Of Intracranial Structure
|
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Hemangioma Of Intracranial Structures
|
|
|
| Telangiectasis |
|
|
| Cardiofaciocutaneous Syndrome 1 |
|
Cardiofaciocutaneous Syndrome
|
Cfc Syndrome
|
|
Cardio-Facio-Cutaneous Syndrome
|
CFC1
|
|
Cfcs
|
Cardio-Facial-Cutaneous Syndrome
|
|
Congenital Heart Defects Characteristic Facial Appearance Ectodermal Abnormalities And Growth Failure
|
Cardiofaciocutaneous Syndrome, Type 1
|
|
|
| Leukemia, Chronic Myeloid |
|
Chronic Myeloid Leukemia
|
Chronic Myelogenous Leukemia
|
|
CML
|
Chronic Granulocytic Leukemia
|
|
Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib
|
Chronic Myeloid Leukaemia
|
|
Chronic Granulocytic Leukaemia
|
Chronic Myelogenous Leukaemia
|
|
Myeloid Leukemia, Chronic
|
Leukemia, Chronic Myelogenous
|
|
Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic
|
Cml - Chronic Myelogenous Leukemia
|
|
Cgl
|
Chronic Myelocytic Leukemia
|
|
Leukemia, Chronic Myeloid, Atypical
|
ACML
|
|
Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative
|
Myeloid Leukemia Chronic
|
|
Leukemia, Myeloid, Chronic
|
Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative
|
|
Cml- [Chronic Myeloid Leukaemia]
|
Cgl - [Chronic Granulocytic Leukaemia]
|
|
Chronic Myelocytic Leukaemia
|
|
|
| Nevus, Epidermal |
|
Epidermal Nevus
|
Woolly Hair Nevus
|
|
Epidermal Naevus
|
Epidermal Nevus Syndrome
|
|
Nevus, Keratinocytic, Nonepidermolytic
|
Epidermal Nevus, Somatic
|
|
Nevus, Epidermal, Somatic
|
Nevus Sebaceous Or Woolly Hair Nevus, Somatic
|
|
Nonepidermolytic Keratinocytic Nevus
|
Epidermal Hamartoma Syndrome
|
|
Wooly Hair Nevus
|
Keratinocytic Non-Epidermolytic Nevus
|
|
KNEN
|
Pigmented Moles
|
|
Organoid Nevus Phakomatosis
|
Nevus Sebaceous
|
|
Melanocytic Nevus
|
Melanocytic Nevus Of Skin
|
|
|
| Costello Syndrome |
|
Faciocutaneoskeletal Syndrome
|
Fcs Syndrome
|
|
Congenital Myopathy With Excess Of Muscle Spindles
|
CSTLO
|
|
CMEMS
|
Fcss
|
|
Myopathy, Congenital, With Excess Of Muscle Spindles
|
|
|
| Capillary Lymphangioma |
|
Microcystic Lymphatic Malformation
|
Capillary Lymphatic Malformation
|
|
Microcystic Infiltrating Lymphatic Malformation
|
Microcystic Lymphangioma
|
|
Superficial Lymphangioma
|
Cutaneous Lymphangioma Circumscriptum
|
|
Superficial Lymphatic Malformation
|
Cutaneous Lymphangioma
|
|
Lymphangioma Of Skin
|
Lymphangioma Circumscriptum
|
|
|
| Infiltrating Angiolipoma |
|
Angiolipoma, Infiltrating
|
|
|
| Gingival Fibromatosis |
|
Hereditary Gingival Fibromatosis
|
Hereditary Gingival Hyperplasia
|
|
Autosomal Dominant Gingival Fibromatosis
|
Autosomal Dominant Gingival Hyperplasia
|
|
Fibromatosis, Gingival, Hereditary
|
Fibromatosis, Gingival
|
|
|
| Noonan Syndrome 1 |
|
Noonan Syndrome
|
NS1
|
|
Male Turner Syndrome
|
Female Pseudo-Turner Syndrome
|
|
Turner Phenotype With Normal Karyotype
|
Noonan Syndrome With Pigmented Villonodular Synovitis
|
|
Turner'S Phenotype, Karyotype Normal
|
Familial Turner Syndrome
|
|
Noonan'S Syndrome
|
Noonan-Ehmke Syndrome
|
|
Ns
|
Pseudo-Ullrich-Turner Syndrome
|
|
Turner Syndrome In Female With X Chromosome
|
Turner-Like Syndrome
|
|
Ullrich-Noonan Syndrome
|
Noonan-Like/Multiple Giant Cell Lesion Syndrome
|
|
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
|
Pterygium Colli Syndrome
|
|
Noonan Syndrome, Type 1
|
Turner Syndrome, Male
|
|
|
